Schusterova Petra, Mudronova Dagmar, Penazziova Katarina Loziakova, Hajduckova Vanda, Csank Tomas
Department of Microbiology and Immunology, University of Veterinary Medicine and Pharmacy in Košice, Košice, Slovak Republic.
Vet Med (Praha). 2024 May 27;69(5):169-176. doi: 10.17221/106/2023-VETMED. eCollection 2024 May.
This study aimed to evaluate the immunomodulatory effect of the probiotic L26 Biocenol (L26) and its purified exopolysaccharide (EPS) with respect to antiviral innate immune response. In our experiment, we used porcine epithelial IPEC-J2 cells as a model of the intestinal barrier in a homologous infection by porcine strain OSU6 (RVA). The production of selected molecules of non-specific humoral immunity was evaluated at the mRNA level. The EPS alone significantly increased the level of interferon λ3 (IFN-λ3) mRNA in the non-infected IPEC-J2 cells ( < 0.001). We also tested whether the treatment of IPEC-J2 cells by L26 or EPS influences the replication of RVA by virus titration and real-time PCR. We found that a pre-treatment in combination with subsequent continuous stimulation has no influence on the RVA replication. However, both treatments significantly decreased the RVA-induced production of IFN-λ3 ( < 0.05) and the "SOS" cytokine interleukin 6 (IL-6; < 0.01), already at the transcription level. In addition, the EPS treatment resulted in significantly increased IL-10 mRNA in the RVA-infected cells. In summary, we assume an immunoregulatory potential of L26 Biocenol and its EPS in the local intestinal antiviral immune response.
本研究旨在评估益生菌L26 Biocenol(L26)及其纯化的胞外多糖(EPS)对病毒先天性免疫反应的免疫调节作用。在我们的实验中,我们使用猪上皮IPEC-J2细胞作为肠道屏障模型,用于猪轮状病毒株OSU6(RVA)的同源感染。在mRNA水平评估了非特异性体液免疫所选分子的产生。单独的EPS显著增加了未感染的IPEC-J2细胞中干扰素λ3(IFN-λ3)mRNA的水平(<0.001)。我们还通过病毒滴定和实时PCR测试了用L26或EPS处理IPEC-J2细胞是否会影响RVA的复制。我们发现,预处理与随后的持续刺激相结合对RVA复制没有影响。然而,两种处理均在转录水平上显著降低了RVA诱导的IFN-λ3产生(<0.05)和“SOS”细胞因子白细胞介素6(IL-6;<0.01)。此外,EPS处理导致RVA感染细胞中IL-10 mRNA显著增加。总之,我们推测L26 Biocenol及其EPS在局部肠道抗病毒免疫反应中具有免疫调节潜力。